| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNATrp gene
|
Silvestri, G.
|
|
1998
|
8 |
5 |
p. 291-295
5 p.
|
artikel
|
| 2 |
A novel γ-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy
|
van der Kooi, A.J
|
|
1998
|
8 |
5 |
p. 305-308
4 p.
|
artikel
|
| 3 |
Distal myopathy with rimmed vacuoles
|
Nonaka, Ikuya
|
|
1998
|
8 |
5 |
p. 333-337
5 p.
|
artikel
|
| 4 |
Genetic heterogeneity in Miyoshi-type distal muscular dystrophy
|
Linssen, W.H.J.P
|
|
1998
|
8 |
5 |
p. 317-320
4 p.
|
artikel
|
| 5 |
Immunocytochemical detection of emerin within the nuclear matrix
|
Squarzoni, S
|
|
1998
|
8 |
5 |
p. 338-344
7 p.
|
artikel
|
| 6 |
Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families
|
Barth, Peter G
|
|
1998
|
8 |
5 |
p. 296-304
9 p.
|
artikel
|
| 7 |
Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological features
|
Cupler, Edward J
|
|
1998
|
8 |
5 |
p. 321-326
6 p.
|
artikel
|
| 8 |
Overview of distal myopathies: from the clinical to the molecular
|
Barohn, Richard J
|
|
1998
|
8 |
5 |
p. 309-316
8 p.
|
artikel
|
| 9 |
Threshold expression of the tRNALys A8344G mutation in single muscle fibres
|
Moslemi, Ali-Reza
|
|
1998
|
8 |
5 |
p. 345-349
5 p.
|
artikel
|
| 10 |
Tibial muscular dystrophy – from clinical description to linkage on chromosome 2q31
|
Udd, Bjarne
|
|
1998
|
8 |
5 |
p. 327-332
6 p.
|
artikel
|
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